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DC Field | Value | Language |
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dc.contributor.author | Marković, Violeta | - |
dc.contributor.author | Eric Slavica | - |
dc.contributor.author | Juranić Z. | - |
dc.contributor.author | Stanojkovic, Tatjana | - |
dc.contributor.author | Joksović, Ljubinka | - |
dc.contributor.author | Ranković B. | - |
dc.contributor.author | Kosanic, Marijana | - |
dc.contributor.author | Joksović, Milan | - |
dc.date.accessioned | 2021-04-20T14:47:17Z | - |
dc.date.available | 2021-04-20T14:47:17Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0045-2068 | - |
dc.identifier.uri | https://scidar.kg.ac.rs/handle/123456789/10068 | - |
dc.description.abstract | A series of aminomethylidene derivatives obtained from 4-formyledaravone were synthesized and characterized by IR, NMR and elemental analysis. All the compounds were screened for their antitumor activity. The compound containing 5-phenylpyrazole moiety (3q) exhibited remarkable antitumor activity in in vitro assays, especially against human breast cancer MDA-MB-361 and MDA-MB-453 cell lines. The most important whole-molecule descriptors for antitumor activity on MDA-MB-453 cells belong to the group of quantum-chemical descriptors. © 2010 Elsevier Inc. All rights reserved. | - |
dc.rights | restrictedAccess | - |
dc.source | Bioorganic Chemistry | - |
dc.title | Synthesis, antitumor activity and QSAR studies of some 4-aminomethylidene derivatives of edaravone | - |
dc.type | article | - |
dc.identifier.doi | 10.1016/j.bioorg.2010.10.003 | - |
dc.identifier.scopus | 2-s2.0-78751647459 | - |
Appears in Collections: | Faculty of Science, Kragujevac |
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PaperMissing.pdf Restricted Access | 29.86 kB | Adobe PDF | View/Open |
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